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Detection and Quantification of Plasmodium DNA in Dried Blood Spots Using a Commercial Real-Time PCR Assay and Filter Card System

Authors: Thomas Hanscheid, Vera Codices, Adrian J.F. Luty, Ayola A. Adegnika, Peter G. Kremsner and Martin P. Grobusch
Publication Date: 03 Feb 2009
Human Parasitic Diseases 2009:1 1-4

Thomas Hanscheid1,2, Vera Codices2, Adrian J.F. Luty3, Ayola A. Adegnika1,4,5, Peter G. Kremsner1,5 and Martin P. Grobusch1,6

1Medical Research Unit, Albert Schweitzer Hospital, Lambaréné, Gabon. 2Institute of Molecular Medicine and Institute of Microbiology, Lisbon Medical College, Lisbon, Portugal. 3Department of Medical Microbiology, Radboud University Nijmegen Medical Centre, Nijmegen, The Netherlands. 4Department of Parasitol- ogy, Leiden University Medical Centre, Leiden, The Netherlands. 5Department of Parasitology, Institute of Tropical Medicine, University of Tübingen, Tübingen, Germany. 6Infectious Diseases Unit, Division of Clinical Microbiology and Infectious Diseases, National Health Laboratory Service and School of Pathology, Faculty of Health Sciences, University of the Witwatersrand, Johannesburg, South Africa.

Abstract

Blood collected on FTA® filter cards was analysed qualitatively and quantitatively with real-time PCR and the results compared with expert microscopy performed on-site in Gabon. There was 100% concordance for fresh blood samples. However, correlation of quantitative PCR-results was rather weak (0.52) and reproducibility showed coefficients of variation ranging from 10%–90%.

Categories: Parasites